A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616455



Internal ID20989526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86876134..86884995hg38UCSC Ensembl
chr7:86505450..86514311hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg388862
hg198862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225035
Samples
Known GenesKIAA1324L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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